Scientific Core 1 Scientific Core 1(SC1) provides imaging capabilities that are used broadly throughout the Program Project. The core performs: a) microscopic imaging; b) in vivo thrombosis and angiogenesis models; and c) isolation of cells from mice for ex vivo experiments. Microscopic imaging is by far the major service of this Core. This portion is organized to take advantage of the existing instrumentation and expertise within the Lerner Research Institute of the Cleveland Clinic. The instrumentation includes 6 Leica DM Microscopes, two Leica DMI6000 microscopes for time lapse imaging, a TIRF system, two Leica TCS-SP2 laser scanning confocal microscopes, a Leica SCN 400 slide scanner, a Leica laser microdissection system, LI-COR Odyssey, laser-based scanning system for gels, in-cell Westerns, ELISA/FLISA, EMSA/Gel Shift, Protein Detection, and a new FEI Tecnai G2 Spirit BioTWIN Transmission Electron Microscope equipped with an 11MPix Gatan Orius 832 CCD camera. Beyond the instrumentation is the true expertise of the Core Co-Director, Dr. Judy Drazba, who has more than 20 years of experience in microscopy, hands-on familiarity with all of the instruments and the ability to train investigators from all of the projects in the appropriate use of instrumentation and in the interpretation of data. The in vivo portion of this core performs thrombosis, hemostasis and angiogenesis models in mice. The models to be performed are FeCl3 and rose Bengal induced thrombosis to the mesenteric and carotid arteries, tail bleeding to quantify hemostasis, and matrigel plug and RM-1 prostate tumor as angiogenesis. The portion of the Core is led by Dr. Eugene Podrez, who is experienced in the performance of these models and led a similar and successful core in the previous funding period. The third element of SC1 performs isolation of murine endothelial cells and smooth muscle cells. These cells are used in two of Projects and having these isolations performed by experienced technologists adds to the success of establishing such cultures and the uniformity of behavior of the cells. By providing skilled leadership and organization, SC1 epitomizes the value that can be gained from centralization of key functions and expertise within a Core within the Program Project.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL073311-13
Application #
9258333
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Program Officer
Sarkar, Rita
Project Start
2004-04-15
Project End
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
13
Fiscal Year
2017
Total Cost
$195,587
Indirect Cost
$72,187
Name
Cleveland Clinic Lerner
Department
Type
Domestic Higher Education
DUNS #
135781701
City
Cleveland
State
OH
Country
United States
Zip Code
44195
Szpak, Dorota; Izem, Lahoucine; Verbovetskiy, Dmitriy et al. (2018) ?M?2 Is Antiatherogenic in Female but Not Male Mice. J Immunol 200:2426-2438
Plow, Edward F; Wang, Yunmei; Simon, Daniel I (2018) The search for new antithrombotic mechanisms and therapies that may spare hemostasis. Blood 131:1899-1902
Sossey-Alaoui, Khalid; Pluskota, Elzbieta; Szpak, Dorota et al. (2018) The Kindlin-2 regulation of epithelial-to-mesenchymal transition in breast cancer metastasis is mediated through miR-200b. Sci Rep 8:7360
Gao, Detao; Podrez, Eugene A (2018) Characterization of covalent modifications of HDL apoproteins by endogenous oxidized phospholipids. Free Radic Biol Med 115:57-67
Wang, Yunmei; Gao, Huiyun; Shi, Can et al. (2017) Leukocyte integrin Mac-1 regulates thrombosis via interaction with platelet GPIb?. Nat Commun 8:15559
Meller, Julia; Chen, Zhihong; Dudiki, Tejasvi et al. (2017) Integrin-Kindlin3 requirements for microglial motility in vivo are distinct from those for macrophages. JCI Insight 2:
Hirbawi, Jamila; Bialkowska, Katarzyna; Bledzka, Kamila M et al. (2017) The extreme C-terminal region of kindlin-2 is critical to its regulation of integrin activation. J Biol Chem 292:14258-14269
Ithychanda, Sujay S; Dou, Kevin; Robertson, Stephen P et al. (2017) Structural and thermodynamic basis of a frontometaphyseal dysplasia mutation in filamin A. J Biol Chem 292:8390-8400
Feng, Weiyi; Valiyaveettil, Manojkumar; Dudiki, Tejasvi et al. (2017) ?3 phosphorylation of platelet ?IIb?3 is crucial for stability of arterial thrombus and microparticle formation in vivo. Thromb J 15:22
Plow, Edward F (2017) An enlightening year in vascular biology. Curr Opin Hematol 24:222-223

Showing the most recent 10 out of 105 publications